甲状腺功能减退症视神经病变并发神经脊髓炎谱系障碍:病例报告。

IF 0.5 Q4 OPHTHALMOLOGY
Case Reports in Ophthalmology Pub Date : 2024-08-08 eCollection Date: 2024-01-01 DOI:10.1159/000540496
Teruaki Tokuhisa, Takaaki Hayashi, Shusaku Omoto, Ai Kozaki, Toshu Inoue, Tadashi Nakano
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引用次数: 0

摘要

简介神经脊髓炎视神经谱系障碍(NMOSD)是一种自身免疫性疾病,主要针对中枢神经系统,特别是脊髓和视神经。NMOSD 通常与甲状腺病变有关,如巴塞杜氏病或桥本氏甲状腺炎。甲状腺眼病(TED)是一种自身免疫性疾病,其特征是眼外肌发炎和肥大。甲状腺功能减退性视神经病变(DON)是TED的一种重要并发症,可能导致不可逆的视力丧失。我们报告了一例并发 NMOSD 的 DON 病例:我们报告了一例表现为 DON 的自身免疫性疾病,患者是一名 44 岁的日本女性,曾患巴塞杜氏病,视力下降,眼眶疼痛。脑磁共振成像显示她的直肌肥大,压迫了双侧视神经。因此,她被诊断为 DON,并接受了三个疗程的类固醇半脉冲治疗和左眼眶减压手术,缓解了视神经压迫症状。然而,视力预后仍然不佳。随后的血清学检测显示,aquaporin-4 抗体呈阳性。开始使用白细胞介素-6受体单克隆抗体satralizumab与类固醇联合治疗,以抑制自身免疫反应,降低NMOSD复发风险。治疗后,未再报告NMOSD复发:本病例强调了考虑自身免疫性疾病患者可能同时患有 DON 和 NMOSD 的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dysthyroid Optic Neuropathy Complicated by Neuromyelitis Optica Spectrum Disorder: A Case Report.

Introduction: Neuromyelitis optica spectrum disorder (NMOSD) is an autoimmune disorder that principally targets the central nervous system, specifically the spinal cord and optic nerves. NMOSD is often associated with thyroid pathologies such as Graves' disease or Hashimoto's thyroiditis. Thyroid eye disease (TED) is an autoimmune condition characterized by inflammation and hypertrophy of the extraocular muscles. Dysthyroid optic neuropathy (DON), a critical complication of TED, may lead to irreversible visual loss. We report a case of DON complicated by NMOSD.

Case presentation: We report a case of an autoimmune disease presenting as DON in a 44-year-old Japanese woman with a history of Graves' disease, who experienced reduced visual acuity and orbital pain. Brain magnetic resonance imaging disclosed hypertrophy of the rectus muscles, compressing the optic nerve bilaterally. Consequently, she was diagnosed with DON and underwent three courses of steroid semi-pulse therapy and left orbital decompression surgery, alleviating optic nerve compression. Nevertheless, the visual prognosis remained poor. A subsequent serological test showed positive for aquaporin-4 antibody. Treatment with satralizumab, an interleukin-6 receptor monoclonal antibody, was initiated in conjunction with steroids to suppress the autoimmune response and reduce NMOSD relapse risk. Following this treatment, no NMOSD recurrences were reported.

Conclusion: This case highlights the necessity of considering the possible coexistence of DON and NMOSD in patients with autoimmune diseases.

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来源期刊
CiteScore
0.90
自引率
0.00%
发文量
129
审稿时长
12 weeks
期刊介绍: This peer-reviewed online-only journal publishes original case reports covering the entire spectrum of ophthalmology, including prevention, diagnosis, treatment, toxicities of therapy, supportive care, quality-of-life, and survivorship issues. The submission of negative results is strongly encouraged. The journal will also accept case reports dealing with the use of novel technologies, both in the arena of diagnosis and treatment. Supplementary material is welcomed. The intent of the journal is to provide clinicians and researchers with a tool to disseminate their personal experiences to a wider public as well as to review interesting cases encountered by colleagues all over the world. Universally used terms can be searched across the entire growing collection of case reports, further facilitating the retrieval of specific information. Following the open access principle, the entire contents can be retrieved at no charge, guaranteeing easy access to this valuable source of anecdotal information at all times.
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